chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6127596626127596627TA15GENIChomozygous143993981
6127598130127598131CT21GENIChomozygous143993982
6127598206127598207AT15GENIChomozygous143993983
6127599957127599958CT35GENIChomozygous143993984
6127600208127600209TC28GENIChomozygous143993985
6127600534127600535GT20GENIChomozygous143993986
6127601517127601518CA8GENIChomozygous404000759
6127601517127601518C8GENICheterozygous404000760
6127601682127601683TC16GENIChomozygous143993987
6127605407127605408GA10GENIChomozygous143993988
6127605431127605432CT10GENIChomozygous143993989
6127610393127610394T10GENICheterozygous143977441
6127601519127601520TA8GENIChomozygous404000761
6127601519127601520T8GENICheterozygous404000762
6127602885127602885G28GENIChomozygous143977438
6127604635127604639AAAC23GENICheterozygous143977439
6127605234127605234AGTGCTCCCTCAGACAGTAGACCAG16GENIChomozygous143977440
6127611869127611870GA19GENIChomozygous143993990
6127611939127611940AG19GENIChomozygous143993991
6127612359127612359AGAAAGAGAGAAAGAAAGAAAGAA7GENIChomozygous143977442
6127613271127613272TG10GENIChomozygous143993992